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Phosphatidylethanolamine Improves Postnatal Growth Retardation by Regulating Mucus Secretion of Intestinal Goblet
Nan Wang1,2, Chengming Wang1,2, Ming Qi1,2
1College of Animal Science and Technology, Hunan Agricultural University, Changsha 410128, China.
Insights
Phosphatidylethanolamine (PE) supplementation improved growth in piglets with postnatal growth retardation (PGR). PE enhanced intestinal barrier function, increased MUC2 expression, and promoted goblet cell differentiation, alleviating PGR symptoms.
Area of Science:
- Neonatal nutrition
- Gastroenterology
- Animal science
Background:
- Phosphatidylethanolamine (PE) is a vital phospholipid for neonatal development.
- Postnatal growth retardation (PGR) negatively impacts neonate growth and intestinal health.
- Improving intestinal barrier function is a key strategy to address PGR.
Purpose of the Study:
- To investigate the effects of exogenous Phosphatidylethanolamine (PE) on postnatal growth retardation (PGR) in neonatal pigs.
- To determine if PE supplementation can improve intestinal barrier function in piglets with PGR.
- To elucidate the mechanisms by which PE influences intestinal health and growth.
Main Methods:
- Thirty-two neonatal pigs were divided into control and PE-supplemented groups, with normal birth weight (NBW) and PGR subgroups.
- PE was administered during lactation and post-weaning periods.
- Intestinal morphology, MUC2 expression, goblet cell differentiation (Spdef), and endoplasmic reticulum stress markers were analyzed.
Main Results:
- PE supplementation improved growth performance in PGR piglets compared to controls.
- PGR piglets exhibited damaged intestinal morphology, which PE partially restored by increasing villus height to crypt depth ratio and goblet cell numbers.
- PE increased MUC2 expression and Spdef mRNA levels while reducing endoplasmic reticulum stress markers in PGR piglets.
Conclusions:
- Exogenous Phosphatidylethanolamine (PE) effectively alleviates postnatal growth retardation (PGR) in neonatal pigs.
- PE enhances intestinal barrier function by promoting goblet cell differentiation and MUC2 expression.
- PE supplementation represents a promising strategy for improving neonatal growth and intestinal health.
Abstract:
Phosphatidylethanolamine (PE), a multifunctional phospholipid, is necessary for neonate development. This study aimed to explore the impact of the regulation of exogenous PE on postnatal growth retardation (PGR) by improving intestinal barrier function. Thirty-two neonatal pigs were divided into four groups according to their body weight (BW 2.79 ± 0.50 kg or 1.88 ± 0.40 kg) at 7 days old, CON-NBW, PE-NBW, CON-PGR, and PE-PGR. PE was supplemented to NBW piglets and PGR piglets during lactation and post-weaning periods. Compared with the NBW piglets, the growth performance of PGR piglets was lower, while PE improved the poor growth performance. PGR piglets showed injured intestinal morphology, as evidenced by the reduced ratio of villus height to crypt depth (VH/CD) and goblet cell numbers in the jejunum and ileum. PE recovered the intestinal barrier injury by increasing VH/CD and goblet cell numbers. The decreased MUC2 mRNA and protein expressions were observed in the small intestine of PGR piglets, and PE remarkably increased the expression of MUC2. Mechanistically, PE increased the goblet cell differentiation promoting gene spdef mRNA levels and reduced the mRNA expressions involved in endoplasmic reticulum stress in the jejunal and ileal mucosa of PGR piglets. Overall, we found that PE alleviated growth retardation by regulating intestinal health and generalized its application in neonates.
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